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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1815472Generated: October 29, 2026

2-Chlorobenzaldehyde → HCID 86601532, compound

https://huagongshe.com/reaction/1815472

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChlorobenzaldehydeHCID 6996—
Reactant1,2,3,4-TetrahydroisoquinolineHCID 7046—
Reactant6-Amino-1-hexanolHCID 19960—
Reactant2,4-DichlorobenzenethiolHCID 70730—
Reactant2-BromobenzenethiolHCID 80598—
Reactant3-Chloro-4-fluorobenzaldehydeHCID 593866—
ProductHCID 86601532HCID 86601532—

Reaction Steps

The title compound was prepared by the procedures described in Example 1 substituting 2,4-dichlorothiophenol with 2-bromothiophenol, 2-chlorobenzaldehyde with 3-chloro-4-fluoro-benzaldehyde, and 6-amino-1-hexanol with tetrahydroisoquinoline. 1H NMR (DMSO-d6, 300 MHz) δ 8.12 (d, J=7.4 Hz, 1H), 7.81 (dd, J=7.7, 1.1 Hz, 1H), 7.67 (dd, J=8.3, 1.3 Hz, 1H), 7.47 (m, 2H), 7.43 (dd, J=7.5, 1.3 Hz, 2H), 7.34 (dt, J=7.6, 1.7 Hz, 1H), 7.27 (d 7.7 Hz, 1H), 7.19 (m, 4H), 7.05 (d, J=8.1 Hz, 1H), 4.92 (s, 1H), 4.72 (s, 1H), 3.95 (t, J=5.9 Hz, 1H), 3.78 (t, J=5.7 Hz, 1H), 2.89 (t, J=5.3 Hz, 1H), 2.83 (t, J=3.7, 1H). HRMS calculated for C24H19N1O2S1Br1Cl1: 484.0138. Observed: 484.0128.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06878700B1
Source datasetuspto-grants-2005_04
ORD IDord-fcc937dd2f314d21b6c569b443f64fe3
Source noteuspto-grants-2005_04